Method for Splitting Carbon Dioxide into Molecular Oxygen and Carbon

ABSTRACT

Apparatus and methods for facilitating an intramolecular reaction that occurs in single collisions of CO 2  molecules (or their derivatives amenable to controllable acceleration, such as CO 2   +  ions) with a solid surface, such that molecular oxygen (or its relevant analogs, e.g., O 2   +  and O 2   −  ions) is directly produced are provided. The reaction is driven by kinetic energy and is independent of surface composition and temperature. The methods and apparatus may be used to remove CO 2  from Earth&#39;s atmosphere, while, in other embodiments, the methods and apparatus may be used to prevent the atmosphere&#39;s contamination with CO 2  emissions. In yet other embodiments, the methods and apparatus may be used to obtain molecular oxygen in CO 2 -rich environments, such as to facilitate exploration of extraterrestrial bodies with CO 2 -rich atmospheres (e.g. Mars).

CROSS-REFERENCE TO RELATED APPLICATIONS

The application is a continuation of U.S. patent application Ser. No. 15/905,708, filed, Feb. 26, 2018, entitled “Method for Splitting Carbon Dioxide into Molecular Oxygen and Carbon,” which claims priority to U.S. Provisional Application No. 62/463,021, filed Feb. 24, 2017, entitled “Method for Splitting Carbon Dioxide into Molecule Oxygen and Carbon,” the disclosures of which are incorporated herein by reference in their entireties.

STATEMENT OF FEDERAL SUPPORT

This invention was made with government support under Grant No. PHY1202567 awarded by the National Science Foundation. The government has certain rights in the invention.

FIELD OF THE INVENTION

Apparatus and methods for producing molecular oxygen (or its relevant analogs, e.g., O₂ ⁺ and O₂ ⁻ ions) directly from CO₂ molecules are provided.

BACKGROUND OF THE INVENTION

Carbon dioxide (CO₂) is a symmetric linear triatomic molecule, wherein carbon atom is covalently bound to two oxygen atoms via strong double bonds. Trace amounts of CO₂, a colorless gas, occur naturally in the Earth's atmosphere, wherein its current concentration is ˜0.04% (405 ppm) by volume, having risen from pre-industrial levels of 280 ppm. However, despite a seemingly low concentration, CO₂ gas is the main contributor to the atmospheric greenhouse effect, and, therefore, is of major concern to humanity, especially in view of the alarmingly rapid increases of its atmospheric concentration in recent decades. Consequently, various technologies for CO₂ sequestration from the Earth's atmosphere are currently being investigated and pursued, although no definitive solution has been found to date.

In contrast, dioxygen gas (O₂) is the basis of life on Earth and is rather abundant in the atmosphere. However, an oxygen-rich atmosphere is quite unique to Earth, because, although elemental oxygen is the third most abundant element in the universe, its molecular dioxygen form is very rare. Specifically, in contrast to Earth, where oxygenic photosynthesis has made O₂ abundant, interstellar and cometary oxygen atoms are chemically bound to other elements in compounds such as H₂O, CO₂, CO, silicates, and metal oxides, making the release of O₂ from these reservoirs difficult and energetically very expensive. As such, only tenuous amounts of dioxygen are found elsewhere in our solar system, e.g., in the moons of Jupiter and Saturn and on Mars; in fact, the abundance of molecular oxygen has been suggested as a promising biomarker. Accordingly, efficient generation of O₂ from CO₂ is particularly desirable for space travel to Mars, Venus, and other planetary bodies with CO₂-rich atmospheres.

SUMMARY OF THE INVENTION

Embodiments are directed to methods and apparatus for forming molecule oxygen from carbon dioxide molecules.

In many embodiments the methods for splitting carbon dioxide into molecular oxygen and carbon include accelerating carbon dioxide molecules against a solid surface at an incident angle such that the carbon dioxide molecules have kinetic energy E₀ of between 10 and 300 eV at collision against the solid surface.

In other embodiments the method further includes accelerating the carbon dioxide molecules prior to the acceleration. In other such embodiments the carbon dioxide molecules are ionized by one of either photoexcitation or energetic electron bombardment.

In still other embodiments the accelerated carbon dioxide molecules have a kinetic energy of between 20 and 200 eV.

In yet other embodiments the carbon dioxide molecules subjected to acceleration are produced in a carbon dioxide plasma. In some such embodiments the plasma ionizes the carbon dioxide molecules to produce carbon dioxide ions, and wherein the potential of the plasma is externally adjusted to produce an electric field in the plasma such that the carbon dioxide ions are accelerated to the kinetic energy E₀.

In still yet other embodiments the solid surface comprises grounded metal electrodes.

In still yet other embodiments the solid surface comprises one or more element selected from the group: any element of rows 4, 5, and 6 of the Periodic table, an oxide of any element thereof, any combination thereof.

In still yet other embodiments the solid surface comprises one or more element selected from the group: Ti, V, Cr, Mn, Fe, CO, Ni, Cu, Zn, Ge, Y, Zr, Nb, Mo, Ru, Rh, Pd, Ag, In, Sn, Sb, Te, Ce, Hf, Ta, Re, Os, Ir, Pt, Au, Pb, Bi, an oxide of any element thereof, any combination thereof.

In still yet other embodiments the solid surface is selected from the group of silicon oxide or indium tin oxide.

In still yet other embodiments the acceleration occurs via application of an electric field.

In still yet other embodiments the conversion efficiency of carbon dioxide molecules to molecular oxygen is up to 33%.

In still yet other embodiments the conversion efficiency of carbon dioxide molecules to molecular oxygen is at least 5%.

Many other embodiments are directed to an apparatus for splitting carbon dioxide into molecular oxygen and carbon, including:

-   -   a source of a gaseous mixture comprising carbon dioxide gas,     -   a solid surface,     -   a molecular accelerator configured to selectively accelerate the         carbon dioxide molecules against the solid surface at an         incident angle, such that the kinetic energy of the carbon         dioxide molecules at collision against the solid surface is         between 10 and 300 eV.

In other embodiments the apparatus further includes an ionizer for ionizing the carbon dioxide molecules prior to the acceleration, and wherein the molecular accelerator comprises an electric field.

In still other embodiments the carbon dioxide molecules are ionized by one of either photoexcitation or energetic electron bombardment.

In yet other embodiments the accelerated carbon dioxide molecules have a kinetic energy of between 20 and 200 eV.

In still yet other embodiments the carbon dioxide molecules subjected to acceleration are produced in a carbon dioxide plasma. In some such embodiments the plasma ionizes the carbon dioxide molecules to produce carbon dioxide ions, and wherein the potential of the plasma is externally adjusted to produce an electric field in the plasma such that the carbon dioxide ions are accelerated to the kinetic energy E₀.

In still yet other embodiments the solid surface comprises one or more grounded metal electrodes.

In still yet other embodiments the solid surface comprises one or more biased metal electrodes.

In still yet other embodiments the solid surface is selected form the group consisting of any element of rows 4, 5, and 6 of the Periodic table, an oxide of any element thereof, any combination thereof.

In still yet other embodiments the solid surface is selected form the group consisting of Ti, V, Cr, Mn, Fe, CO, Ni, Cu, Zn, Ge, Y, Zr, Nb, Mo, Ru, Rh, Pd, Ag, In, Sn, Sb, Te, Ce, Hf, Ta, Re, Os, Ir, Pt, Au, Pb, Bi, an oxide of any element thereof, any combination thereof.

In still yet other embodiments the solid surface is selected form the group of silicon oxide or indium tin oxide.

In still yet other embodiments the conversion efficiency of carbon dioxide molecules to molecular oxygen is up to 33%.

In still yet other embodiments the conversion efficiency of carbon dioxide molecules to molecular oxygen is at least 5%

Additional embodiments and features are set forth in part in the description that follows, and in part will become apparent to those skilled in the art upon examination of the specification or may be learned by the practice of the disclosed subject matter. A further understanding of the nature and advantages of the present disclosure may be realized by reference to the remaining portions of the specification and the drawings, which forms a part of this disclosure.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features and advantages of the present invention will be better understood by reference to the following detailed description when considered in conjunction with the accompanying data and figures, wherein:

FIGS. 1a-c summarize scattering dynamics of the three molecular ion products (CO₂ ⁺ in FIG. 1 a, O₂ ⁺ in FIG. 1 b, and O₂ ⁻ in FIG. 1c ) resulting from CO₂ ⁺ collisions with Au surface in accordance with embodiments of the application.

FIGS. 2a-d provide spectra confirming the presence of fragmentation products in CO₂ ⁺ collisions with Au surface in accordance with embodiments of the application.

FIG. 3a schematically illustrates the collision sequence of an accelerated linear CO₂ molecule scattering on surface, in accordance with embodiments of the application. FIG. 3b provides data summarizing a kinematic analysis of the collision sequence depicted in FIG. 3 a.

FIGS. 4a-b illustrate a velocity analysis (a) and estimation of the CO₂* excitation energy (b) for scattered CO₂ dissociation products in accordance with embodiments of the application.

FIG. 5 provides data showing the trend in O₂ formation vs. partial dissociation in CO₂ ⁺/Au collisions in accordance with embodiments of the application.

FIGS. 6a-c illustrate energy distributions of CO₂ ⁺ (a), O₂ ⁺ (b), and O₂ ⁻ (c) ion exits from CO₂ ⁺/Pt collisions as a function of the respective product exit energy for various CO₂ ⁺ beam energies (E₀), in accordance with embodiments of the application.

FIGS. 7a-d illustrate energy distributions of dissociation fragments from CO₂ ⁺/Pt collisions, in accordance with embodiments of the application.

FIG. 8 illustrates energy distributions of O₂ ⁻ ions scattered from CO₂ ⁺/SiOx collisions, as a function of the CO₂ ⁺ incidence energy, in accordance with embodiments of the application.

DETAILED DISCLOSURE

Turning to the drawings and data, methods and apparatus for the facile conversion of CO₂ to molecular oxygen are provided. It will be understood that the embodiments of the invention described herein are not intended to be exhaustive or to limit the invention to precise forms disclosed. Rather, the embodiments selected for description have been chosen to enable one skilled in the art to practice the invention.

Despite the pressing demand for effective removal of CO₂ from the atmosphere and apparent benefits of converting CO₂ specifically into O₂, only one abiotic pathway to O₂ was known until recently, namely, the three-body recombination reaction, O+O+M→O₂+M, where the requisite atomic oxygen arises from CO₂ photo-dissociation and M is a third body (Kasting, J. F., Liu, S. C., Donahue, T. M. Oxygen levels in the prebiological atmosphere. J. Geophys. Res. 84, 3097-3107 (1979); and Segura, A., Measows, V. S., Kasting, J. F., Crisp, D., Cohen, M. Abiotic formation of O₂ and O₃ in high-CO₂ terrestrial atmospheres. Astron. Astrophys. 472, 665-679 (2007); the disclosures of which are incorporated herein by reference). This finding was superseded by the discovery of two new pathways for direct O₂ formation from CO₂: one via vacuum ultraviolet (VUV) photo-dissociation (as described in Lu, Z., Chang, Y. C., Yin, Q. Z., Ng, C. Y. & Jackson, W. M. Evidence for direct molecular oxygen production in CO₂ photodissociation. Science 346, 61-64 (2014), the disclosure of which is incorporated herein by reference) and one via dissociative electron attachment (DEA) (as described in Wang, X. D., Gao, X. F., Xuan, C. J. & Tian, S. X. Dissociative electron attachment to CO₂ produces molecular oxygen. Nature Chem. 8, 258-263 (2016), the disclosure of which is incorporated herein by reference). In both of these latter studies, direct detection of the neutral O₂ photoproduct was not possible because of background interference. Instead, experimental evidence for the dissociation reaction of a highly-excited CO₂ electronic state (Suits, A. G. & Parker, D. H. Hot molecules-off the batten path. Science 346, 30 (2014), the disclosure of which is incorporated herein by reference) into the C(³P)+O₂(X³Σg⁻) products was based on detecting the complementary atomic C⁺ or C⁻ fragment. In addition, O₂ ⁺ ions from the photo-dissociation of CO₂ were recently detected using strong laser fields to photo-produce the doubly-ionized CO₂ ⁺⁺ state, which dissociates into C⁺+O₂ ⁺, altogether a very inefficient process (Larimian, S. et al. Molecular oxygen observed by direct photoproduction from carbon dioxide. Phys. Rev. A 95, 011404 (2017), the disclosure of which is incorporated herein by reference). Direct production of O₂ ⁻ from dissociative attachment in CO₂ has collision cross sections so small (˜10⁻²⁴ cm²) that “signal must be accumulated over several days” to observe it even with extremely sensitive detection systems (Spence, D. & Schulz, G. J. Cross sections for production of O₂ ⁻ and C⁻ by dissociative electron attachment in CO₂: an observation of the Renner-Teller effect. J. Chem. Phys. 60, 216-220 (1974), the disclosure of which is incorporated herein by reference). Therefore, new methods for the efficient splitting of CO₂ to produce O₂ are highly desirable and sought after in areas ranging from atmospheric science to space travel.

Direct conversion of CO₂ into molecular oxygen is an energetically very unfavorable reaction. In principle, direct dissociation of CO₂ can proceed along three pathways (shown below with the indicated dissociation energies):

CO₂→CO+O (5.5 eV)   (I)

CO₂→C+O₂ (5.8 eV)   (II)

CO₂→C+2O (11.0 eV)   (III)

Channel (I) describes the primary partial dissociation reaction, which has been widely studied in photochemistry and in heterogeneous catalysis under thermal activation conditions (as detailed, for example, in: Rosen, B. A. et al. Ionic liquid-mediated selective conversion of CO₂ to CO at low overpotentials. Science 334, 643-644 (2011); and Liu, M. et al. Enhanced electrocatalytic CO₂ reduction via field-induced reagent concentration. Nature 537, 382-386 (2016), the disclosures of which are incorporated herein by reference). Channel (III) represents the energetically expensive complete dissociation of CO₂ with cleavage of both C—O bonds. In contrast, channel (II) is an exotic pathway, which requires extensive intramolecular bond rearrangement within the triatomic CO₂, despite the fact that its dissociation energy is only 0.3 eV larger than that of channel (I). However, simulations have shown a possible way to realize channel (II) by first forming the cyclic CO₂ complex [c-CO₂(¹A₁)], which then must transform into the collinear COO(¹Σ⁺) intermediate on its way to dissociation into C+O₂. The first step in this scheme requires bending of the linear CO₂ molecule in order to bring the two O atoms in close proximity. Although inaccessible by thermal activation, the barrier to bending may be, in theory, overcome by other means of excitation, such as VUV photon irradiation or energetic electron bombardment.

It has now been discovered that, as described in the embodiments of this invention, channel (II) can also be activated by energetic collisions of CO₂ molecules (or, in some embodiments, of their CO₂ ⁺ ion analogs) with solid surfaces. In many such embodiments, when CO₂ ⁺ ions are collided with a solid surface, O₂ molecules and O₂ ^(±) ions evolve directly from a scattered excited state (CO₂*) undergoing late fragmentation. Accordingly, this application is directed to embodiments of an unexpected and surprisingly efficient method for facilitating an intramolecular reaction that occurs in single collisions of CO₂ molecules (or their derivatives amenable to controllable acceleration, such as CO₂ ⁺ ions) with a solid surface, such that molecular oxygen (or its relevant analogs, e.g., O₂ ⁺ and O₂ ⁻ ions) is directly produced. In many embodiments of the invention, the reaction is driven by momentum of the CO₂ molecule or ion accelerated against a surface and incoming at an incident angle and will occur irrespective of the surface composition and temperature. However, in many embodiments, the yield of O₂ production from CO₂ splitting does depend on surface composition in so far as surfaces that would be reactive with CO₂ or its fragmentation products can poison the reaction. In some embodiments, the method may be used to remove CO₂ from Earth's atmosphere, while, in other embodiments, the method may be used to prevent the atmosphere's contamination with CO₂ emissions. In yet other embodiments, the method may be used to obtain molecular oxygen in CO₂-rich environments, such as to facilitate exploration of extraterrestrial bodies with CO₂-rich atmospheres (e.g. Mars).

In many embodiments, the method for splitting carbon dioxide into molecular oxygen and carbon comprises accelerating molecules of CO₂ to a specific desired velocity, such that the accelerated molecules collide with a solid surface with kinetic energies between 10 and 300 eV. It will be understood that, within this kinetic energy range, the actual amount of energy required for the optimum conversion to O₂ is determined by such parameters as the angle at which the accelerated CO₂ molecule or ion approaches the surface prior to the collision and the atomic mass of the surface atoms. In many embodiments, larger kinetic energies are required to facilitate the reaction for larger angles of incidence θ with respect to the surface normal vector, wherein the least amount of required energy corresponds to normal incidence. More specifically, in many embodiments, if E₀ is the required kinetic energy for maximum conversion at an angle of incidence θ, then the corresponding energy for normal incidence would be E₀ cos²θ.

Without being bound by any theory, the kinematic analysis of the collisional process suggests that CO₂ collisions with the provided surface under the disclosed herein conditions extensively perturb the CO₂ intramolecular triatomic geometry and produce a strongly bent CO₂ excited state, which, subsequently, dissociates to yield molecular as well as ionized O₂. The disclosed herein process is reminiscent of exotic photochemical pathways for CO₂ decomposition, but, unlike any known pathway, which typically have very low O₂ yields, the intramolecular CO₂ decomposition conducted according to the embodiments of this invention has an estimated O₂ yield of ˜33±3%. For comparison, the yield of previously reported CO₂ photo-dissociation pathways is ˜5±2%.

Of course, it will be understood that any acceleration technique known in the art can be employed to bring CO₂ molecules to the velocities and surface striking energies necessary to enable the method of this application. Several approaches are known in the art to produce positively charged CO₂ ions and to controllably accelerate them with an applied electric field. Accordingly, in many embodiments, prior to acceleration, the CO₂ molecules are ionized via photo-excitation with ultraviolet light. In some other embodiments, the CO₂ molecules are ionized by means of energetic electron bombardment under low pressure. In yet other, preferred embodiments, CO₂ plasma is used to produce CO₂ ⁺, which are accelerated against a biased surface with appropriate energy. In yet another embodiment, the solid surface may be moving against heated CO₂ molecules at the required velocity.

In many embodiments, O₂ ions are directly produced in hyperthermal CO₂ ⁺ collisions against Au surfaces. Specifically, FIGS. 1a to 1c summarize exemplary scattering dynamics of such CO₂ ⁺/surface collisions, by showing energy distributions for three of its molecular ion products: CO₂ ⁺ (FIG. 1a ), O₂ ⁺ (FIG. 1b ), and O₂ ⁻ (FIG. 1c ) for various CO₂ ⁺ beam energies (E₀) (as annotated on each panel), and shows that both O₂ ions are detected at certain, relatively narrow energy ranges, along with some amount of survived CO₂ ⁺. Accordingly, first, FIG. 1a shows that a very weak scattered CO₂ ⁺ signal is detected at beam energies (E₀) below 100 eV. Furthermore, the scattered CO₂ ⁺ ion exit energy varies in proportion to the CO₂ ⁺ incidence energy, thus precluding physical sputtering as its origin. Observing dynamic CO₂ ⁺ signal is important because it proves that some CO₂ survives the collision. In addition, the observed kinematics provide insight into the collision sequence of the constituent atoms of the triatomic molecule impinging onto the metal surface. Second, in FIGS. 1b and 1c a strong scattered O₂ signal is observed in both charge polarities, O₂ ⁺ and O₂ ⁻. Here, in contrast to the O₂ ⁻ energy spectra, the O₂ ⁺ signal appears somewhat noisy, owing to detector (channeltron) operation. As observed for the scattered CO₂ ⁺, the O₂ ⁺ and O₂ ⁻ ion exit energies increase monotonically with the CO₂ ⁺ incidence energy. For both polarities, the scattered O₂ ion signal intensity goes through a maximum, then it dies out for E₀>150 eV. Interestingly, the O₂ ⁺ energy spectra develop a shoulder at ˜20 eV for beam energies greater than 100 eV due to physical sputtering. As noted above, the O₂ ⁺ and O₂ ⁻ spectra intensities cannot be directly compared due to differences in how the detector is biased.

Notably, the demonstrated O₂ formation is unexpected, since collision-induced dissociation of CO₂ ⁺ is expected to occur via channel (I) at low collision energies, followed up by channel (III) at larger incidence energies. Indeed, FIGS. 2a-d show that all of the CO₂ ⁺ dissociation products: CO⁺, O⁺, O⁻, and C⁺, are detected in CO₂ ⁺/Au collisions. Furthermore, the exit energies of the CO⁺ and O⁻ peaks vary with incidence energy (FIGS. 2a and 2c ), indicating they are produced dynamically within the surface collision. However, as will be shown below, these fragments originate from the same excited state as the one producing the O₂ ions. In contrast, the position of the O⁺ and C⁺ peaks is almost invariant around 20 eV (Exit Energy), suggesting a different origin. The appearance of scattered C⁺ products for E₀>70 eV confirms that complete dissociation of CO₂ via channel (III) also occurs.

Since scattered CO₂ ⁺ ions are detected along with other collision products, a fraction of the incident ions must survive the hard collision. The kinematics (described in Yao, Y. & Giapis, K. P. Kinematics of Eley-Rideal reactions at hyperthermal energies. Phys. Rev. Lett. 116, 253202 (2016), the disclosure of which is incorporated herein by reference) of the scattered CO₂ ⁺ ions can help elucidate the scattering mechanism, which in turn provides clues for the formation of O₂. Accordingly, FIG. 3a schematically illustrates the collision sequence of a linear CO₂ molecule scattering on a solid surface according to many embodiments of this invention. In this scheme, the leading O atom collides with the surface first, followed by collision of the complementary CO moiety, and further followed by the molecule bending during the hard collision and forming of an excited triangular state, which, in turn, undergoes late dissociation into C+O₂.

FIG. 3b provides ion exit energies of CO₂ ⁺, O₂ ⁺, O₂ ⁻, CO⁺, O⁻, and C⁺ ions as a function of CO₂ ⁺ incidence energy, along with corresponding one-parameter linear fittings as solid lines. Here, the slope for CO₂ ⁺ is calculated from binary collision theory (BCT), assuming two sequential collisions as proposed in the scheme depicted in FIG. 3 a; while the other slopes are calculated by assuming a common excited CO₂ precursor state fragmenting spontaneously into daughter ions. It should be noted, that since the O₂ ⁺ exit energy data overlaps with the O₂ data, only the linear fitting for O₂ ⁻ is shown in FIG. 3 b. In view of the data presented in FIG. 3b , first, if CO₂ ⁺ scatters as a whole molecule (i.e., a hard sphere with atomic mass of 44 Dalton), BCT predicts a kinematic factor of 0.6349, which does not fit well the energy data shown in FIG. 3 b. This is not surprising given the quasi-linear triatomic nature of the CO₂ ⁺ ion (as explained in Walsh, A. D. The electronic orbitals, shapes, and spectra of polyatomic molecules. Part II. Non-hydride AB₂ and BAC molecules J. Chem. Soc., 2266-2288 (1953); and Grimm, F. A. & Larsson, M. A Theoretical Investigation of the Low Lying Electronic States of CO₂ ⁺ in Both Linear and Bent Configurations. Phys. Scr. 29, 337-343 (1984); the disclosures of which are incorporated herein by reference). The next plausible scattering model assumes that parts of the molecular ion suffer distinct and successive collisions without molecular dissociation (as depicted in FIG. 3a ): first the leading O atom collides with a surface Au atom, then the remaining CO moiety collides with the same Au atom. This model is similar to how diatomic molecules scatter on metal surfaces (as described, for example in Yao, Y. & Giapis, K. P. Direct hydrogenation of dinitrogen and dioxygen via Eley-Rideal reactions. Angew. Chem. Int. Ed. 55, 11595-11599 (2016), the disclosure of which is incorporated herein by reference). Applying BCT to the sequential collision scattering model yields a kinematic factor of 0.7870, which fits perfectly the CO₂ ⁺ exit energy data provided in FIG. 3 b. This scattering behavior has been verified for another quasi-linear molecular ion, NO₂ ⁺, when scattering on Au surfaces (described in Pfeiffer, G. V. & Allen, L. Electronic structure and geometry of NO₂ ⁺ and NO₂ ⁻ . J. Chem. Phys. 51, 190-202 (1969), the disclosure of which is incorporated herein by reference).

Accordingly, in many embodiments, facilitating energetic CO₂ ⁺ scattering against a biased surface affects the angular configuration of the CO₂ molecule during the collision and results in the unexpectedly efficient O₂ production. Although not to be bound by theory, according to the disclosed herein mechanism and for many CO₂ approach geometries, one of the O atoms of the CO₂ molecule collides with the surface first and then rebounds in closer proximity to the other O atom in the resulting CO moiety. This mechanical deformation of the CO₂ molecule is equivalent to a bending mode but occurs at much faster timescales than vibronic interactions (Renner-Teller effect). In addition, electronic excitation may also occur during the hard collision (as explained in Mace, J., Gordon, M. J. & Giapis, K. P. Evidence of simultaneous double-electron promotion in F+ collisions with surfaces. Phys. Rev. Lett. 97, 257603 (2006), the disclosure of which is incorporated herein by reference). Therefore, according to many embodiments, a strongly bent, highly excited CO₂* state is produced in CO₂/surface collision, which next decomposes preferentially into C+O₂ on the rebound from the surface. Furthermore, in some embodiments, charge exchange of the CO₂ dissociation fragments with the surface may aide the ionization of the O₂ (FIG. 3a ). In other embodiments, the excited state may split directly into ion pairs.

Furthermore, the very weak signal observed for CO₂ ⁺ scattered according to the embodiments of the invention implies a very low survival probability. CO₂ ⁺ fragmentation can occur before, during, or after the hard collision with the surface. Only delayed fragmentation, for example, of a rebounding highly excited CO₂* precursor state, can explain dissociation products having the same exit velocity as the precursor. Therefore, according to some embodiments, the kinematic factors of O₂, CO and O products can be calculated from energy conservation to be 0.5724, 0.5008, and 0.2862, respectively. The linear O₂ ⁻, CO⁺ and O⁻ ion exit data are fitted very well with these kinematic factors as slopes (FIG. 3b ). However, the O⁺ and C⁺ data cannot be fitted linearly, wherein their broader distributions suggest that other processes, such as surface sputtering, contribute to the measured peaks at lower energies, rendering de-convolution of the contribution from excited CO₂* difficult.

According to many embodiments and the observed kinematics of the ion exits from CO₂ ⁺ scattering on Au, molecular O₂ ions originate in surviving CO₂ molecules or ions, possibly highly excited. To further illustrate this process, the distributions of the CO₂ ⁺, O₂ ⁺, O₂ ⁻, CO⁺ and O⁻ ion exits for E₀=56.4 eV are re-plotted in FIG. 4a as a function of the corresponding ion exit velocity. As seen in FIG. 4a , the exit velocities of scattered CO⁺, O₂ ⁺ and O₂ ⁻ line up very well, thus confirming the single precursor origin, while the O⁻ peak is somewhat broader than the latter three and overlaps partially with the O₂ ion exit peaks. Surprisingly, the surviving CO₂ ⁺ is clearly faster than the O₂ ion products. Therefore, the CO₂* undergoing post-collisional dissociation according to the embodiments of the invention must become internally excited by inelastic processes, which, in turn, robs kinetic energy from the incident CO₂ ⁺ and results in its slower exit. Although the putative CO₂* state cannot be directly detected, the additional energy needed to produce it can be estimated by assuming that the daughter O₂ ⁻ ion is emitted with the CO₂* exit velocity. Then, the kinetic energy difference between CO₂ ⁺ and CO₂* can be estimated and should be a measure of the relative excitation energy. Accordingly, FIG. 4b summarizes the results of this simple calculation as a function of E₀. Notably, for E₀<70 eV, the relative excitation energy is about 6 eV—a value remarkably close to that required for CO₂ partial dissociation according to channel (I) mechanism, or for direct O₂ formation according to channel (II) mechanism. Coincidentally, the energy penalty to form the triangular CO₂ state (¹A₁) is also 6 eV (as reported in Lu, Z., Chang, Y. C., Yin, Q. Z., Ng, C. Y. & Jackson, W. M. Evidence for direct molecular oxygen production in CO₂ photodissociation, Science 346, 61-64 (2014), the disclosure of which is incorporated herein by reference). For E₀ above 70 eV, the relative excitation energy increases while the scattered CO₂ ⁺ signal dies out (FIG. 1a ). Simultaneously, C⁺ ions become detectable suggesting the onset of complete dissociation via channel (III).

Due to the violence of the surface collision, even the surviving CO₂ molecular ions can be highly excited. The intercept of the CO₂ ⁺ data fitting in FIG. 3b reflects the inelastic energy loss for the CO₂ ⁺ ion exit, which amounts to 8.69 eV—most of it going to internal excitation. Adding the inelastic energy loss of the surviving CO₂ ⁺, the absolute excitation energy for the CO₂* precursor could be as high as 14 eV. This energy is comparable to the VUV-photon and electron energy needed for the direct formation of O₂ from CO₂.

An important question for the CO₂ ⁺ dissociation reaction into O₂ is that of efficiency. One way to assess the efficiency of CO₂ dissociation according to the embodiments of the application is in terms of selectivity of channel (II) versus the predominant channel (I). Kinematic analysis has shown that the CO⁺, O₂ ⁻ and O⁻ products are directly formed from a common parent, the putative CO₂* excited precursor state. At low CO₂ ⁺ incidence energies, the main dissociation pathways are: a) partial dissociation to form CO+O (channel (I)), and b) intramolecular reaction to form O₂+C (channel (II)). Assuming that O₂ ⁻ and O⁻ are formed by resonant electron transfer to the corresponding neutrals with the same efficiency, one can use the relative intensity of O₂ ⁻ and O⁻ to estimate the selectivity for O₂ formation, S(O₂), defined as follows:

${{S\left( O_{2} \right)} = \frac{I\left( O_{2}^{-} \right)}{{I\left( O_{2}^{-} \right)} + {I\left( O^{-} \right)}}},$

where I is the intensity of the corresponding negative ion exits. Notably, the electron affinities of O atoms and O₂ are 1.46 eV and 0.45 eV, respectively, wherein the difference implies that negative ion formation should be more efficient for O than for O₂, due to the lower barrier to resonant electron attachment. Therefore, S(O₂), as defined here, underestimates the actual O₂ formation selectivity. Furthermore, at high CO₂ ⁺ incidence energy, channel (III) also opens up, doubling the number of O atoms and O⁻ ions produced and, thus, further worsening the estimate for O₂ formation selectivity. With these limitations in mind, one can obtain a conservative estimate of the O₂ formation selectivity, which is plotted in FIG. 5 as a function of CO₂ ⁺ incidence energy. According to the data plotted in FIG. 5, the O₂ formation selectivity increases with E₀, goes through a maximum of ˜33±3% at E₀=70 eV, then decreases. The first increase is consistent with more energy available for direct O₂ formation. Remarkably, the turnaround point coincides with the opening up of the complete dissociation channel.

Although the above discussed results are based on monitoring ionic products, it is well known in ion-surface collisions, that the majority (˜98%) of the ions are neutralized by the surface prior to the collision and thus collide with the surface as neutrals, in this case neutral (uncharged) CO₂. Likewise, many scattered CO₂ molecules and products of CO₂ dissociation will not be charged, nevertheless will be contributing to the O₂ yield.

The direct O₂ production by collisional activation of CO₂ ⁺ according to the embodiments of the application is clearly more efficient than activation using other means, such as high-energy photons or electrons. Indeed, O₂ formation by photo-excitation of CO₂ has an estimated selectivity of only 5±2% vs. the partial dissociation channel, while DEA processes in CO₂ have minuscule cross sections for O₂ production. In many embodiments, the higher O₂ selectivity in the collisional activation process is attributed to more facile structural rearrangement in the CO₂ during the hard collision, which brings the two O atoms closer together.

In some embodiments, the atomic composition of the collision surface affects the O₂ yield of CO₂ splitting method of the application and must be optimized. Specifically, in many embodiments, surfaces that can be easily sputtered, i.e., where the surface erodes significantly at low incidence energy, or where carbon atoms stick preferentially to the surface to form coatings, are not desirable, as they can interfere with the surface excitation process that facilitates the reaction and poison the CO₂ dissociation. Consequently, in many embodiments, the general requirement for the collision surface is that it contains an atom with atomic mass larger than 16-18 Dalton, which is the atomic mass of the elemental oxygen, including its isotopes. In many preferred embodiments, the atomic mass of the collision surface elements is between 20 and 200 Dalton. Furthermore, although surfaces comprising atoms with atomic mass larger than 20 Dalton are acceptable, surfaces comprising atoms with atomic mass heavier than 40 Dalton are preferred. In many embodiments, the collision surface comprises of one or more element found in rows 4, 5, and 6 of the Periodic table or such element's oxide. In some such embodiments, the collision surface is comprised of one or more element from the list: Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ge, Y, Zr, Nb, Mo, Ru, Rh, Pd, Ag, In, Sn, Sb, Te, Cd, Hf, Ta, Re, Os, Ir, Pt, Au, Pb, Bi, an oxide of any element thereof, or any combination thereof. In contrast, in many embodiments, surfaces comprising certain elements that might interfere with the CO₂ dissociation reaction must be avoided. For example, surfaces comprising tungsten (W) must be avoided in many embodiments, as such surfaces, when oxidized, form a volatile tungsten oxide that vaporizes and consumes the surface.

Furthermore, in many embodiments, the collision enabled CO₂ splitting reaction is generic to metal surfaces (FIGS. 6 and 7), and occurs even on oxides (FIG. 8). Specifically, FIGS. 6 and 7 demonstrate that, in some embodiments, efficient splitting of CO₂ into O₂ can be achieved via CO₂ collisions with Pt surfaces, while FIG. 8 shows that, in other embodiments, the similar behavior is observed in CO₂ collisions with silicon oxide surfaces.

In many embodiments, the CO₂ splitting method of the instant application may be exploited in plasma reactors, wherein ion/wall collisions occur spontaneously at energies determined by the plasma potential. Remarkably, past attempts at using CO₂ plasmas were plugged by relatively low O₂ conversion, ostensibly because of the slow kinetics for the two-step O₂ formation process in gas-phase collisions (as detailed in Spencer, L. F. & Gallimore, A. D. Efficiency of CO₂ dissociation in a radio-frequency discharge. Plasma Chem. Plasma Phys. 31, 79-89 (2010), the disclosure of which is incorporated herein by reference). However, according to the embodiments of the invention, the O₂ yield is greatly improved with the following three modifications to plasma reactor methods of CO₂ splitting: a) maximizing the CO₂ ⁺ ion density, b) tuning the plasma potential between 40 and 150 eV, and c) providing grounded metal electrodes to enable CO₂ ⁺ ion/surface collisions.

Exemplary Embodiments/Experimental Materials and Methods

The following example sets forth certain selected embodiments relate to the above disclosure. It will be understood that the embodiments presented in this section are exemplary in nature and are provided to support and extend the broader disclosure, these embodiments are not meant to confine or otherwise limit the scope of the invention.

All experiments described in the instant application were carried out in a custom-made low-energy ion scattering apparatus described in detail in Gordon, M. J. & Giapis, K. P. Low-energy ion beam line scattering apparatus for surface science investigations. Rev. Sci. Instrum. 76, 083302 (2005), the disclosure of which is incorporated herein by reference. The CO₂ ⁺ ion beam was extracted from an inductively-coupled plasma, struck in a reactor held at 2 mTorr using a CO₂/Ar/Ne gas mixture supplied with 500 W RF power at 13.56 MHz. Ions delivered to a grounded surface at 45° incidence angle; typical beam currents of 5 to 15 μA were spread over a ˜3 mm spot. Beam energy was varied between 40-200 eV by externally adjusting the plasma potential. Typical target surfaces were polycrystalline Au foils (5N), sputter-cleaned with an Ar⁺ ion gun before each run. Scattered ion products, exiting at an angle of 45° in the scattering plane, were energy- and mass-resolved using an electrostatic ion energy analyzer and a quadruple mass spectrometer, respectively. All ions were detected using a channel electron multiplier, biased as appropriate to detect positive or negative ions. Differences in detector bias precluded a direct comparison of signal intensities between product ions of different charge polarities. All collected signals were normalized to the beam current measured on the sample.

DOCTRINE OF EQUIVALENTS

This description of the invention has been presented for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise form described, and many modifications and variations are possible in light of the teaching above. The embodiments were chosen and described in order to best explain the principles of the invention and its practical applications. This description will enable others skilled in the art to best utilize and practice the invention in various embodiments and with various modifications as are suited to a particular use. The scope of the invention is defined by the following claims. 

1. A method for splitting carbon dioxide into molecular oxygen and carbon, comprising accelerating carbon dioxide molecules against a solid surface at an incident angle such that the carbon dioxide molecules have kinetic energy E₀ of between 10 and 300 eV at collision against the solid surface.
 2. The method of claim 1, further comprising ionizing the carbon dioxide molecules prior to the acceleration.
 3. The method of claim 2, wherein the carbon dioxide molecules are ionized by one of either photoexcitation or energetic electron bombardment.
 4. The method of claim 1, wherein the accelerated carbon dioxide molecules have a kinetic energy of between 20 and 200 eV.
 5. The method of claim 1, wherein the carbon dioxide molecules subjected to acceleration are produced in a carbon dioxide plasma.
 6. The method of claim 5, wherein the plasma ionizes the carbon dioxide molecules to produce carbon dioxide ions, and wherein the potential of the plasma is externally adjusted to produce an electric field in the plasma such that the carbon dioxide ions are accelerated to the kinetic energy E₀.
 7. The method of claim 1, wherein the solid surface comprises grounded metal electrodes.
 8. The method of claim 1, wherein the solid surface comprises one or more element selected from the group: any element of rows 4,5, and 6 of the Periodic table, an oxide of any element thereof, any combination thereof.
 9. The method of claim 1, wherein the solid surface comprises one or more element selected from the group: Ti, V, Cr, Mn, Fe, CO, Ni, Cu, Zn, Ge, Y, Zr, Nb, Mo, Ru, Rh, Pd, Ag, In, Sn, Sb, Te, Ce, Hf, Ta, Re, Os, Ir, Pt, Au, Pb, Bi, an oxide of any element thereof, any combination thereof.
 10. The method of claim 1, wherein the solid surface is selected from the group of silicon oxide or indium tin oxide.
 11. The method of claim 1, wherein the acceleration occurs via application of an electric field.
 12. The method of claim 1, wherein the conversion efficiency of carbon dioxide molecules to molecular oxygen is up to 33%.
 13. The method of claim 1, wherein the conversion efficiency of carbon dioxide molecules to molecular oxygen is at least 5%.
 14. An apparatus for splitting carbon dioxide into molecular oxygen and carbon, comprising: a source of a gaseous mixture comprising carbon dioxide gas, a solid surface, a molecular accelerator configured to selectively accelerate the carbon dioxide molecules against the solid surface at an incident angle, such that the kinetic energy of the carbon dioxide molecules at collision against the solid surface is between 10 and 300 eV.
 15. The apparatus of claim 11, further comprising an ionizer for ionizing the carbon dioxide molecules prior to the acceleration, and wherein the molecular accelerator comprises an electric field.
 16. The apparatus of claim 12, wherein the carbon dioxide molecules are ionized by one of either photoexcitation or energetic electron bombardment.
 17. The apparatus of claim 11, wherein the accelerated carbon dioxide molecules have a kinetic energy of between 20 and 200 eV.
 18. The apparatus of claim 11, wherein the carbon dioxide molecules subjected to acceleration are produced in a carbon dioxide plasma.
 19. The apparatus of claim 15, wherein the plasma ionizes the carbon dioxide molecules to produce carbon dioxide ions, and wherein the potential of the plasma is externally adjusted to produce an electric field in the plasma such that the carbon dioxide ions are accelerated to the kinetic energy E₀.
 20. The apparatus of claim 11, wherein the solid surface comprises one or more grounded metal electrodes. 